Issue 0, 1971

The chemistry of fungi. Part LXI. The synthesis of (±)-sclerotiorin, of (±)-4,6-dimethylocta-trans-2,trans-4-dienoic acid, and of an analogue of rotiorin

Abstract

Syntheses of (±)-sclerotiorin, the principal pigment of several fungi including Penicillium multicolor and P. sclerotiorum, of (±)-4,6-dimethylocta-trans-2,trans-4-dienoic acid [a major degradation product of (+)- and of (–)-sclerotiorin] and of (+)-5-chloroisorotiorin, an angular analogue of rotiorin, are described.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 3566-3571

The chemistry of fungi. Part LXI. The synthesis of (±)-sclerotiorin, of (±)-4,6-dimethylocta-trans-2,trans-4-dienoic acid, and of an analogue of rotiorin

R. Chong, R. R. King and W. B. Whalley, J. Chem. Soc. C, 1971, 3566 DOI: 10.1039/J39710003566

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